نتایج جستجو برای: richner
تعداد نتایج: 33 فیلتر نتایج به سال:
The association of herpetoid corneal changes with circumscribed palmo-plantar keratoderma was first described by Richner (I938). Hanhart (1947) suggested that this represented a recessively inherited ectodermal syndrome, and the condition is sometimes called the Richner-Hanhart syndrome. Subsequent reports have been relatively few: Cremona (I 957); Kuske (I959); Franceschetti and Thier (I96I); ...
BARBARA TSCHIRREN*, VERENA SALADIN*, PATRICK S. FITZE†, HUBERT SCHWABL‡ and HEINZ RICHNER* * Evolutionary Ecology Group, Zoological Institute, University of Bern, 3012 Bern, Switzerland; † Behavioural Ecology Group, Zoology Department, University of Cambridge, Cambridge CB2 3EJ, UK; and ‡ School of Biological Sciences, Centre for Reproductive Biology, Washington State University, Pullman, WA 99...
PIERRE BIZE*, ALEXANDRE ROULIN†, JOSÉ L. TELLA‡, LOUIS-FÉLIX BERSIER§ and HEINZ RICHNER* *Institute of Zoology, University of Bern, Baltzerstrasse 6, 3012 Bern, Switzerland; †Department of Ecology & Evolution, University of Lausanne, Biology Building, 1015 Lausanne, Switzerland; ‡Department of Applied Biology, Estación Biológica de Doñana, Pabellón del Perú, Avda. M. Luisa s/n, E-41013 Sevilla,...
Correction: Zika virus has oncolytic activity against glioblastoma stem cells Zhe Zhu, Matthew J. Gorman, Lisa D. McKenzie, Jiani N. Chai, Christopher G. Hubert, Briana C. Prager, Estefania Fernandez, Justin M. Richner, Rong Zhang, Chao Shan, Eric Tycksen, Xiuxing Wang, Pei-Yong Shi, Michael S. Diamond, Jeremy N. Rich, and Milan G. Chheda Vol. 214, No. 10, October 2017. https://doi.org/10.1084/...
tyrosinemia type ii is a rare autosomal recessive disorder wich can present itself with recurrent epithelial keratitis, hyperkeratotic skin lesions and mental retardation. this article reports the rare occurrence of this disease in both offsprings (two brothers) of a family (consanguinous'marriage) who were managed with a lowprotein diet and a special regimen.
We report three cases from two unrelated families of infants with arthrogryposis multiplex congenita, cholestatic jaundice, and renal Fanconi's syndrome. In both families the parents were consanguineous. All three children died by 7 months of age. This association was first reported in 1973 by Lutz-Richner and Landolt and again in another family by Nezelof et al in 1979. However, because of dif...
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